100156-45-4 Usage
Uses
Used in Flavor and Fragrance Industry:
(2,2,3-Trimethylcyclopent-3-enyl)methanol is used as a flavor and fragrance ingredient for its pleasant, floral scent. It is incorporated into various products such as perfumes, soaps, and cosmetics to enhance their aroma and appeal to consumers.
Used in Organic Synthesis:
(2,2,3-Trimethylcyclopent-3-enyl)methanol is utilized in the synthesis of other organic compounds, contributing to the development of new chemical products and materials.
Used in Antimicrobial Applications:
Due to its antimicrobial properties, (2,2,3-Trimethylcyclopent-3-enyl)methanol has potential use in the development of antimicrobial products. Its ability to inhibit the growth of microorganisms could be beneficial in creating sanitizing and cleaning agents.
However, it is important to exercise caution when using and handling (2,2,3-Trimethylcyclopent-3-enyl)methanol, as its safety profile and potential health effects are not fully understood. Further research and testing are necessary to ensure its safe and effective application in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 100156-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100156-45:
(8*1)+(7*0)+(6*0)+(5*1)+(4*5)+(3*6)+(2*4)+(1*5)=64
64 % 10 = 4
So 100156-45-4 is a valid CAS Registry Number.
100156-45-4Relevant articles and documents
MICROBIOLOGICAL TRANSFORMATIONS-XV; MICROBIOLOGICAL TRANSFORMATIONS OF 1-(2,2,3-TRIMETHYLCYCLOPENT-3-EN-YL)-PROPAN-2-ONE AND THEIR HOMOLOGUES BY ACREMONIUM ROSEUM s.s. GAMS 1971
Siewinski, A.,Dmochowska-Gladysz, J.,Kolek, T.,Zabza, A.,Derdzinski, K.,Nespiak, A.
, p. 2265 - 2270 (2007/10/02)
The microbiological transformations of 1-(2,2,3-trimethylcyclopent-3-en-yl)-propan-2-one (2a) and its four (2b-e) homologues by Acremonium roseum were investigated.For 2a, b and e ketones Baeyer-Villiger oxydation was predominant reaction, but ketone 2c and d were mainly hydroxylated.
